Canonical Allele Identifier: CA138337530

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43531807T>C , CM000668.2:g.43531807T>C GRCh38
NC_000006.11:g.43499545T>C , CM000668.1:g.43499545T>C GRCh37
NC_000006.10:g.43607523T>C NCBI36
NG_028283.3:g.27106T>C
NG_051658.1:g.49269A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265351.12:c.2444-232A>G (XPO5) MANE Select ENSP00000265351.7:n.2444-232A>G
ENST00000607635.2:c.*4+2448T>C (POLR1C) ENSP00000496683.1:n.*4+2448T>C
ENST00000643341.1:c.922+10759T>C (POLR1C) ENSP00000496018.1:n.922+10759T>C
ENST00000646433.1:c.922+10759T>C (POLR1C) ENSP00000494368.1:n.922+10759T>C
ENST00000646700.1:c.922+10759T>C (POLR1C) ENSP00000495521.1:n.922+10759T>C
ENST00000265351.11:c.2444-232A>G (XPO5) ENSP00000265351.7:n.2444-232A>G
ENST00000398835.7:c.490-232A>G (XPO5)
NM_020750.2:c.2444-232A>G (XPO5) NP_065801.1:n.2444-232A>G
XM_011515000.1:c.922+10759T>C (POLR1C) XP_011513302.1:n.922+10759T>C
NM_001363658.1:c.922+10759T>C (POLR1C) NP_001350587.1:n.922+10759T>C
NR_144392.1:n.2793-232A>G (XPO5)
NM_020750.3:c.2444-232A>G (XPO5) MANE Select NP_065801.1:n.2444-232A>G
NM_001363658.2:c.922+10759T>C (POLR1C) NP_001350587.1:n.922+10759T>C
NM_001318876.2:c.945+2536T>C (POLR1C) NP_001305805.1:n.945+2536T>C
NR_144392.2:n.2756-232A>G (XPO5)